2 Amino 5 Methyl Thiophene 3 Carboxylic Acid Methyl Ester
quinoline thiophene imidazole thiazole

2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER

Taiy Chemical

    Specifications

    HS Code

    830573

    Chemical Formula C7H9NO2S
    Molar Mass 171.217 g/mol
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, dichloromethane
    Melting Point Data may vary, typically in a certain temperature range
    Boiling Point Data may vary, depending on purity and conditions
    Density Data may vary
    Odor May have a characteristic odor

    As an accredited 2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    General Information
    Where to Buy 2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER in China?
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    Frequently Asked Questions

    As a leading 2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC chemical properties of ACID METHYL ESTER
    2-Amino-5-methyl-thiophene-3-carboxylic acid methyl ester, this material has unique chemical properties. Its appearance is often white to off-white crystalline powder, which is due to the orderly arrangement of molecular structures. From the perspective of solubility, it is slightly soluble in water, but soluble in common organic solvents, such as ethanol, acetone, etc. This characteristic is due to the interaction between its molecular polarity and solvent molecules.
    When it comes to chemical stability, it is quite stable when properly stored at room temperature and pressure. In case of strong oxidants or strong acids and bases, its structure is easily damaged. For example, under strong acid conditions, ester groups may hydrolyze to form corresponding carboxylic acids and methanol; in strong alkali environments, amino groups may also react to change the original properties of the molecule.
    In terms of chemical reactivity, amino groups can participate in many nucleophilic reactions, because nitrogen atoms are rich in lone pairs of electrons, which are easy to attack electron-deficient substrates. Ester groups can perform reactions such as ester exchange, showing rich chemical change possibilities. This compound plays an important role in the field of organic synthesis and is often used as a key intermediate for the preparation of more complex thiophene-containing drugs or functional materials, laying the foundation for many chemical synthesis pathways and opening the door to a variety of compounds.
    2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC the main uses of ACID METHYL ESTER
    2-Amino-5-methyl-thiophene-3-carboxylic acid methyl ester has a wide range of uses and has its own impact in the field of chemical and pharmaceutical.
    In the chemical industry, it can be a key raw material for organic synthesis. Due to its unique molecular structure, it contains amino, methyl, thiophene ring and ester group, and various functional groups endow it with various reactivity. Other organic compounds containing thiophene structure can be prepared by esterification, amidation, substitution and other reactions. These compounds may have specific photoelectric properties and have potential applications in the manufacture of organic optoelectronic materials, such as Light Organic Emitting Diode (OLED) and organic solar cells. Thiophene compounds are often used as electron transport layers or photosensitive materials to improve device performance.
    In the pharmaceutical field, 2-amino-5-methyl-thiophene-3-carboxylic acid methyl esters also play an important role. Because its structure is similar to some active molecules in vivo, it can participate in the construction of drug molecules. Or to build the core skeleton of the drug, it is modified to enhance the affinity of the drug with the target and improve the drug efficacy. And thiophene ring is often associated with biological activity in pharmaceutical chemistry, which can increase the lipid solubility of the drug, help it pass through the biofilm, and improve the bioavailability. Many antibacterial, anti-inflammatory and anti-tumor drugs are developed with thiophene-containing compounds as precursors, which may provide a key basis for the development of new drugs.
    In short, methyl 2-amino-5-methyl-thiophene-3-carboxylate, with its unique structure, provides possibilities and opportunities for the creation of new functional materials and drugs in the chemical and pharmaceutical fields.
    2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC is the synthesis method of ACID METHYL ESTER
    To prepare 2-amino-5-methyl-thiophene-3-carboxylic acid methyl ester, you can follow the following ancient method.
    First take 5-methyl-thiophene-3-carboxylic acid, which is the starting material. Place it in a reactor, add an appropriate amount of methanol, which is the key reagent for providing methyl. Add concentrated sulfuric acid with a catalyst amount. Concentrated sulfuric acid acts as a catalyst here, which can accelerate the process of esterification reaction. The temperature should be carefully controlled, and the reaction temperature should be maintained between 60 and 80 ° C by water bath or oil bath. This temperature range is suitable for esterification reaction. The reaction lasts about 3-5 hours (4-6 hours), during which time stirring should be continued to allow the reactants to fully contact and promote the completion of the reaction.
    After the reaction is completed, the reaction liquid is cooled to room temperature. Subsequently, the cooled reaction liquid is poured into a container containing an appropriate amount of ice water to terminate the reaction and allow the product to precipitate. At this time, the product may contain unreacted raw materials, catalysts and by-products. To purify the product, an organic solvent such as ether or ethyl acetate can be used for extraction. After multiple extractions, the organic phases are combined.
    The organic phase is then washed with a saturated sodium bicarbonate solution, which removes unreacted acid and residual sulfuric acid. After washing, the organic phase is dried with anhydrous sodium sulfate to remove the moisture contained in it. Finally, by vacuum distillation, the organic solvent is removed, and the fractions in a specific boiling point range are collected to obtain pure 2-amino-5-methyl-thiophene-3-carboxylic acid methyl ester.
    Another method is to convert 5-methyl-thiophene-3-carboxylic acid into acyl chloride, react with thionyl chloride, and under mild heating conditions, the acid chloride product can be obtained for several hours (2-3 hours). After that, the acid chloride is mixed with methanol and an appropriate amount of acid binding agent such as triethylamine, and the acid chloride reacts with methanol to form the target product 2-amino-5-methyl-thiophene-3-carboxylic acid methyl ester. The acid binding agent can neutralize the hydrogen chloride generated by the reaction and promote the positive progress of the reaction. Subsequent steps also need to be extracted, washed, dried and distilled to purify the product.
    2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC precautions when storing ACID METHYL ESTER
    Methyl 2-amino-5-methyl-thiophene-3-carboxylate is a fine chemical. When storing, many important items need to be paid attention to.
    Choose the first environment. This chemical should be stored in a cool, dry and well-ventilated place. If the ambient temperature is too high, it may cause its chemical properties to change and cause decomposition; if the humidity is too high, or the substance is damp, it will affect the purity and quality. And good ventilation can disperse harmful gases that may evaporate and avoid accumulation and risk.
    Furthermore, the packaging must be in good condition. Damage to the packaging can easily cause substances to leak, and contact with air, moisture, etc. will accelerate deterioration. It should be ensured that the packaging container is made of suitable materials, has good tolerance to the chemical, and does not chemically react with it.
    At the same time, pay attention to isolation from other substances. This chemical should not be mixed with oxidants, acids, alkalis, etc. Because of its active chemical nature, contact with these substances or react violently, and even cause serious consequences such as combustion and explosion.
    Storage areas should also be marked with obvious warning signs to remind personnel of their danger. And regular inspections should be made to check whether the packaging is damaged, whether the substance has deteriorated, etc., so as to detect and deal with problems in time. In this way, the safety and quality of methyl 2-amino-5-methyl-thiophene-3-carboxylate during storage can be ensured.
    2-AMINO-5-METHYL-THIOPHENE-3-CARBOXYLIC the market price range of ACID METHYL ESTER
    I don't know the market value of "2 - AMINO - 5 - METHYL - THIOPHENE - 3 - CARBOXYLIC ACID METHYL ESTER". This is a chemical product, and its market value is often affected by many factors. First, the degree is of paramount importance, and the high degree will be higher than the low degree. Second, the supply and demand price also has an impact. If you want it, there will be a shortage of it, and the price will rise automatically. On the contrary, the supply and demand will decrease, and the cost of production will also affect the price. The cost of raw materials and manufacturing will all affect the cost, which will make the market different. And due to the difference in sales regions and sales channels, the price will also fluctuate. Or in some places, due to factors such as cost and cost, the price will vary. Therefore, if you want to know the market value, you need to check the chemical raw material trading platform, provide chemical products to suppliers, or check the recent market transactions, so as to obtain the market value.